renal magnesium wasting Gene Set

Dataset HPO Gene-Disease Associations
Category disease or phenotype associations
Type phenotype
Description High urine magnesium in the presence of hypomagnesemia. (Human Phenotype Ontology, HP_0005567)
External Link http://compbio.charite.de/hpoweb/showterm?id=HP:0005567
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Genes

5 genes associated with the renal magnesium wasting phenotype by mapping known disease genes to disease phenotypes from the HPO Gene-Disease Associations dataset.

Symbol Name
CLDN16 claudin 16
CLDN19 claudin 19
FXYD2 FXYD domain containing ion transport regulator 2
IFT122 intraflagellar transport 122
SLC12A3 solute carrier family 12 (sodium/chloride transporter), member 3